Neuroscience Center, UNC Chapel Hill, NC, USA.
Department of Cell Biology and Physiology, UNC Chapel Hill, NC, 27599-7250, USA.
FEBS J. 2019 Sep;286(17):3276-3298. doi: 10.1111/febs.14970. Epub 2019 Jul 12.
Apoptosis plays a major role in shaping the developing nervous system during embryogenesis as neuronal precursors differentiate to become post-mitotic neurons. However, once neurons are incorporated into functional circuits and become mature, they greatly restrict their capacity to die via apoptosis, thus allowing the mature nervous system to persist in a healthy and functional state throughout life. This robust restriction of the apoptotic pathway during neuronal differentiation and maturation is defined by multiple unique mechanisms that function to more precisely control and restrict the intrinsic apoptotic pathway. However, while these mechanisms are necessary for neuronal survival, mature neurons are still capable of activating the apoptotic pathway in certain pathological contexts. In this review, we highlight key mechanisms governing the survival of post-mitotic neurons, while also detailing the physiological and pathological contexts in which neurons are capable of overcoming this high apoptotic threshold.
细胞凋亡在胚胎发生过程中塑造发育中的神经系统方面起着重要作用,因为神经元前体分化为有丝分裂后神经元。然而,一旦神经元被整合到功能回路中并成熟,它们就会极大地限制通过细胞凋亡死亡的能力,从而使成熟的神经系统在整个生命周期中保持健康和功能状态。这种在神经元分化和成熟过程中对细胞凋亡途径的严格限制是由多种独特的机制定义的,这些机制可更精确地控制和限制内在的细胞凋亡途径。然而,尽管这些机制对于神经元的存活是必要的,但成熟的神经元仍然能够在某些病理情况下激活细胞凋亡途径。在这篇综述中,我们强调了控制有丝分裂后神经元存活的关键机制,同时详细说明了神经元能够克服这种高细胞凋亡阈值的生理和病理情况。